Canonical Allele Identifier: CA2580597786

Gene: PHF19

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120878222T>A , CM000671.2:g.120878222T>A	GRCh38
NC_000009.11:g.123640500T>A , CM000671.1:g.123640500T>A	GRCh37
NC_000009.10:g.122680321T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000616568.5:c.43-3466A>T	ENSP00000483946.1:n.43-3466A>T
ENST00000616568.4:c.43-3466A>T	ENSP00000483946.1:n.43-3466A>T
NM_001286840.1:c.43-3466A>T	NP_001273769.1:n.43-3466A>T
XM_011518511.1:c.43-3466A>T	XP_011516813.1:n.43-3466A>T
XM_011518513.1:c.-346-3466A>T	XP_011516815.1:n.-346-3466A>T
XM_011518515.1:c.43-3466A>T	XP_011516817.1:n.43-3466A>T
XM_011518516.1:c.43-3466A>T	XP_011516818.1:n.43-3466A>T
XR_929758.1:n.64-3466A>T
XR_929759.1:n.64-3466A>T
XM_011518511.2:c.43-3466A>T	XP_011516813.1:n.43-3466A>T
XM_011518515.2:c.43-3466A>T	XP_011516817.1:n.43-3466A>T
XM_011518516.2:c.43-3466A>T	XP_011516818.1:n.43-3466A>T
XM_017014612.2:c.-15-3466A>T	XP_016870101.1:n.-15-3466A>T
XM_017014613.1:c.43-3466A>T	XP_016870102.1:n.43-3466A>T
XM_024447505.1:c.-346-3466A>T	XP_024303273.1:n.-346-3466A>T
XR_929758.3:n.574-3466A>T